Enhancement of Cancer Chemotherapeutic Efficacy via Bone-Targeted Drug Delivery Carrier in Bone Metastases

被引:7
|
作者
Xue, Xinghe [1 ,2 ,3 ,4 ]
Yu, Jiachen [1 ,2 ,3 ,4 ]
Lu, Fengfeng [1 ,2 ,3 ,4 ]
Jiang, Hongyi [1 ,2 ,3 ,4 ]
Wang, Xiangyang [1 ,2 ,3 ]
机构
[1] Wenzhou Med Univ, Affiliated Hosp & Yuying Childrens Hosp 2, Dept Orthopaed, Wenzhou 325027, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Sch Med 2, Wenzhou 325027, Zhejiang, Peoples R China
[3] Key Lab Orthopaed Zhejiang Prov, Wenzhou 325027, Zhejiang, Peoples R China
[4] Univ Chinese Acad Sci, Wenzhou Inst, Wenzhou 325011, Zhejiang, Peoples R China
来源
关键词
tumor; metal organic framework; alendronate; doxorubicin; METAL-ORGANIC FRAMEWORKS; ANTICANCER DRUG; GRAPHENE OXIDE; DOXORUBICIN; NANOPARTICLES; ENCAPSULATION; MECHANISMS; PROSTATE; DISEASE; SYSTEMS;
D O I
10.2147/DDDT.S333999
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Purpose: Bone metastases are common in malignant tumors, especially for the advanced cancers. Chemotherapy is an important treatment in clinic, but the application is limited due to the severe adverse reactions. We try to design bone-targeted drug delivery systems (DDS) for the delivery of chemotherapeutic drugs in bone metastatic carcinoma. Material and Methods: We added alendronate (Aln) to metal organic framework (MOF) to synthesize a new bone-targeted DDS named Aln-MOF. Doxorubicin (DOX) as a classic anticancer drug was encapsulated. The material characterization, drug release and bone affinity were detected. In vitro experiment, the cell toxicity was detected by cck-8 test and cellular uptake were detected by laser scanning confocal microscope and flow cytometry. In vivo experiment, the pharmacokinetics of DDS in the blood was analyzed by fluorescence spectrophotometer and the biodistribution was detected by a multi-mode optical in vivo imaging system. The anti-tumor effects of MOFDOX and Aln-MOFDOX were evaluated by monitoring the tumor volume and weight during the animal experiment. In addition, the toxicity of DDS to different organs was determined by HE staining. Results: Aln-MOF showed good stability, no cytotoxicity and better bone affinity than MOF. Both MOFDOX and Aln-MOFDOX could release DOX, and the release rate at pH = 5.5 was faster than the rate at pH = 7.4. The cellular uptake of Aln-MOF and MOF showed no difference. Aln-MOF had a long retention time in blood, which is beneficial for the enrichment of Aln-MOF in tumor sites. Aln-MOF mainly concentrated at bone metastases in mice. MOFDOX and Aln-MOFDOX could effectively delay tumor progression, and the effect of Aln-MOFDOX was more obvious (P < 0.05). Conclusion: Our study confirmed that Aln-MOF has good stability, bone targeting and biosafety. Aln-MOFDOX could release DOX and effectively kill tumor cells of bone metastases. Aln-MOFDOX has a promising prospect in the treatment of bone metastasis.
引用
收藏
页码:4455 / 4468
页数:14
相关论文
共 50 条
  • [21] Novel bone-targeted parathyroid hormone-related peptide antagonists inhibit breast cancer bone metastases
    Ponnapakkam, Tulasi
    Anbalagan, Muralidharan
    Stratford, Robert E., Jr.
    Rowan, Brian G.
    Gensure, Robert C.
    ANTI-CANCER DRUGS, 2021, 32 (04) : 365 - 375
  • [22] Improved Therapeutic Efficacy in Bone and Joint Disorders by Targeted Drug Delivery to Bone
    Takahashi, Tatsuo
    YAKUGAKU ZASSHI-JOURNAL OF THE PHARMACEUTICAL SOCIETY OF JAPAN, 2016, 136 (11): : 1501 - 1508
  • [23] Bone-Targeted Therapy in Early Breast Cancer
    Jerzak, Katarzyna J.
    Raphael, Jacques
    Desautels, Danielle N.
    Blanchette, Phillip S.
    Tyono, Ivan
    Pritchard, Kathleen I.
    ONCOLOGY-NEW YORK, 2018, 32 (11): : 562 - 569
  • [24] Bone-targeted agents and skeletal-related events in breast cancer patients with bone metastases: the state of the art
    Clemons, M.
    Gelmon, K. A.
    Pritchard, K. I.
    Paterson, A. H. G.
    CURRENT ONCOLOGY, 2012, 19 (05) : 259 - 268
  • [25] Bone cement as a local chemotherapeutic drug delivery carrier in orthopedic oncology: A review
    Phull, Sunjeev S.
    Yazdi, Alireza Rahimnejad
    Ghert, Michelle
    Towler, Mark R.
    JOURNAL OF BONE ONCOLOGY, 2021, 26
  • [26] Bone-targeted agent treatment patterns and the impact of bone metastases on patients with advanced breast cancer in the United States
    Henry, David
    von Moos, Roger
    Body, Jean-Jacques
    Rider, Alex
    De Courcy, Jonathan
    Bhowmik, Debajyoti
    Gatta, Francesca
    Hechmati, Guy
    Qian, Yi
    CURRENT MEDICAL RESEARCH AND OPINION, 2019, 35 (03) : 375 - 381
  • [27] Bone-targeted agents in the treatment of lung cancer
    Silva, Shobha C.
    Wilson, Caroline
    Woll, Penella J.
    THERAPEUTIC ADVANCES IN MEDICAL ONCOLOGY, 2015, 7 (04) : 219 - 228
  • [28] Use of Materials Based on Polymeric Silica as Bone-Targeted Drug Delivery Systems for Metronidazole
    Czarnobaj, Katarzyna
    Prokopowicz, Magdalena
    Greber, Katarzyna
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (06):
  • [29] Bone Health and Bone-Targeted Therapies for Nonmetastatic Prostate Cancer RESPONSE
    Alibhai, Shabbir M. H.
    Zukotynski, Katherine
    Walker-Dilks, Cindy
    ANNALS OF INTERNAL MEDICINE, 2018, 168 (06) : 459 - +
  • [30] Peptide-Functionalized Polymers Localize to Resorption Pits for Bone-Targeted Drug Delivery
    Newman, M. R.
    Schmitt, C. S.
    Sheu, T. J.
    Puzas, J. E.
    Benoit, D. S. W.
    TISSUE ENGINEERING PART A, 2014, 20 : S111 - S111